E75.11
Mucolipidosis IV
Approximate Synonyms
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Ganglioside sialidase deficiency
Clinical Information
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An autosomal recessive lysosomal storage disease caused by mutations in the mcoln1 gene. It is characterized by psychomotor developmental delays and ophthalmologic abnormalities.
Details
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E75.11 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
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The 2023 edition of ICD-10-CM E75.11 became effective on October 1, 2022.
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This is the American ICD-10-CM version of E75.11 – other international versions of ICD-10 E75.11 may differ.